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Gene|January 17, 2012
Mosaic down syndrome with a marker: molecular cytogenetic characterization of the marker chromosomeUsha R Dutta, Vijaya Kumar Pidugu, Venkatesh Goud, et al.
Indian Pediatrics|July 14, 2012
Spectrum of Lysosomal storage disorders at a medical genetics center in northern IndiaPrashant K Verma, Prajnya Ranganath, Ashwin B Dalal, et al.
Hemoglobin|April 14, 2018
Compound Heterozygosity for Hb Alperton (HBB: c.407C>T) and IVS-I-5 (G>C) (HBB: c.92+5G>C) Mutations Presenting as a Moderate Anemia in an Indian FamilyKoumudi G Godbole, Angalena Ramachandran, Ashwini S Karkamkar, et al.
The Indian Journal of Medical Research|October 10, 2014
Novel mutations in PRG4 gene in two Indian families with camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndromeRajashree S Nandagopalan, Shubha R Phadke, Ashwin B Dalal, et al.
Indian Heart Journal|October 19, 2016
Brothers with constrictive pericarditis - A novel mutation in a rare diseaseDevendra V Patil, Milind S Phadke, Jivtesh S Pahwa, et al.
Journal of Child Neurology|January 26, 2013
A novel glycine decarboxylase gene mutation in an Indian family with nonketotic hyperglycinemiaJennifer M Love, Debra Prosser, Donald R Love, et al.
Gene|April 2, 2014
Prenatal skeletal dysplasia phenotype in severe MLII alpha/beta with novel GNPTAB mutationShagun Aggarwal, Maria Francisca Coutinho, Ashwin B Dalal, et al.
Indian Heart Journal|November 29, 2008
Association of coronary artery disease with polymorphisms of angiotensin-converting enzyme and methylenetetrahydrofolate reductase geneAshwin B Dalal, Deepshikha Tewari, Satyendra Tewari, et al.
Mitochondrion|February 29, 2024
Mitochondria in biology and medicine - 2023B Disha, Rohan Peter Mathew, Ashwin B Dalal, et al.
Indian Pediatrics|July 24, 2019
Molecular and Histopathological Characterization of Patients Presenting with the Duchenne Muscular Dystrophy Phenotype in a Tertiary Care Center in Southern IndiaKarthik Tallapaka, Prajnya Ranganath, Angalena Ramachandran, et al.
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